FABP7 Regulates Acetyl-CoA Metabolism Through the Interaction with ACLY in the Nucleus of Astrocytes

Author:

Kagawa YoshiteruORCID,Umaru Banlanjo Abdulaziz,Shima Hiroki,Ito Ryo,Zama Ryo,Islam Ariful,Kanno Shin-ichiro,Yasui Akira,Sato Shun,Jozaki Kosuke,Shil Subrata Kumar,Miyazaki Hirofumi,Kobayashi Shuhei,Yamamoto Yui,Kogo Hiroshi,Shimamoto-Mitsuyama Chie,Sugawara Akira,Sugino Norihiro,Kanamori Masayuki,Tominaga Teiji,Yoshikawa Takeo,Fukunaga Kohji,Igarashi Kazuhiko,Owada Yuji

Abstract

AbstractFatty acid binding protein 7 (FABP7) is an intracellular fatty acid chaperon that is highly expressed in astrocytes, oligodendrocyte-precursor cells, and malignant glioma. Previously, we reported that FABP7 regulates the response to extracellular stimuli by controlling the expression of caveolin-1, an important component of lipid raft. Here, we explored the detailed mechanisms underlying FABP7 regulation of caveolin-1 expression using primary cultured FABP7-KO astrocytes as a model of loss of function and NIH-3T3 cells as a model of gain of function. We discovered that FABP7 interacts with ATP-citrate lyase (ACLY) and is important for acetyl-CoA metabolism in the nucleus. This interaction leads to epigenetic regulation of several genes, including caveolin-1. Our novel findings suggest that FABP7-ACLY modulation of nuclear acetyl-CoA has more influence on histone acetylation than cytoplasmic acetyl-CoA. The changes to histone structure may modify caveolae-related cell activity in astrocytes and tumors, including malignant glioma.

Funder

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

GlaxoSmithKline foundation

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

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